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Protoporphyria, Erythropoietic, X-Linked Dominant MeSH Supplementary Concept Data 2022


MeSH Supplementary
Protoporphyria, Erythropoietic, X-Linked Dominant
Unique ID
C567464
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567464
Entry Term(s)
Erythrohepatic Protoporphyria, X-Linked
Xldpt
Registry Number
0
Heading Mapped to
5-Aminolevulinate Synthetase / *deficiency
*Genetic Diseases, X-Linked
*Protoporphyria, Erythropoietic
Frequency
12
Note
mutation in ALAS2
Date of Entry
2012/11/05
Revision Date
2013/11/06
Protoporphyria, Erythropoietic, X-Linked Dominant Preferred
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